Pure Global

"GeneHwa" Enzyme preparations (Non-Sterile) - Taiwan Registration 71c4bb9441489fbc56af5e37e7ea7893

Access comprehensive regulatory information for "GeneHwa" Enzyme preparations (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 71c4bb9441489fbc56af5e37e7ea7893 and manufactured by DNA GENOTEK INC.. The authorized representative in Taiwan is Jinghua Limited.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
71c4bb9441489fbc56af5e37e7ea7893
Registration Details
Taiwan FDA Registration: 71c4bb9441489fbc56af5e37e7ea7893
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"GeneHwa" Enzyme preparations (Non-Sterile)
TW: "่้ฉŠ" ้…ต็ด ่ฃฝๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

71c4bb9441489fbc56af5e37e7ea7893

Ministry of Health Medical Device Import No. 018995

DHA09401899501

Company Information

Canada

Product Details

Limited to the first level identification range of enzyme treatment reagents (B.4400) of the Measures for the Administration of Medical Devices.

B Hematology and pathology devices

B4400 Enzyme Treatment Reagent

Imported from abroad

Dates and Status

Apr 23, 2018

Apr 23, 2023